Canonical Allele Identifier: CA338300782

Gene: PIK3CD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.9715988G>T , CM000663.2:g.9715988G>T	GRCh38
NC_000001.10:g.9776046G>T , CM000663.1:g.9776046G>T	GRCh37
NC_000001.9:g.9698633G>T	NCBI36
NG_023434.1:g.69257G>T , LRG_191:g.69257G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481137.2:c.510G>T	ENSP00000513886.1:p.Gln170His
ENST00000698709.1:c.510G>T	ENSP00000513887.1:p.Gln170His
ENST00000698710.1:c.510G>T	ENSP00000513888.1:p.Gln170His
ENST00000698711.1:n.863G>T
ENST00000698712.1:c.510G>T	ENSP00000513889.1:p.Gln170His
ENST00000698713.1:c.510G>T	ENSP00000513890.1:p.Gln170His
ENST00000698714.1:c.510G>T	ENSP00000513891.1:p.Gln170His
ENST00000698715.1:c.510G>T	ENSP00000513892.1:p.Gln170His
ENST00000698716.1:c.510G>T	ENSP00000513893.1:p.Gln170His
ENST00000698717.1:n.148G>T
ENST00000377346.9:c.510G>T MANE Select	ENSP00000366563.4:p.Gln170His
ENST00000361110.6:c.510G>T	ENSP00000354410.2:p.Gln170His
ENST00000377346.8:c.510G>T	ENSP00000366563.4:p.Gln170His
ENST00000481137.1:n.211G>T
ENST00000536656.5:c.510G>T	ENSP00000446444.2:p.Gln170His
ENST00000543390.2:c.510G>T	ENSP00000443811.2:p.Gln170His
ENST00000628140.2:c.510G>T	ENSP00000486826.1:p.Gln170His
NM_005026.3:c.510G>T , LRG_191t1:c.510G>T	NP_005017.3:p.Gln170His
XM_005263473.1:c.510G>T	XP_005263530.1:p.Gln170His
XM_006710686.1:c.510G>T	XP_006710749.1:p.Gln170His
XM_006710687.1:c.510G>T	XP_006710750.1:p.Gln170His
XM_006710688.1:c.510G>T	XP_006710751.1:p.Gln170His
XM_006710689.1:c.510G>T	XP_006710752.1:p.Gln170His
XM_006710690.1:c.510G>T	XP_006710753.1:p.Gln170His
XM_011541581.1:c.510G>T	XP_011539883.1:p.Gln170His
XM_011541582.1:c.510G>T	XP_011539884.1:p.Gln170His
XR_946667.1:n.719G>T
NM_001350234.1:c.510G>T	NP_001337163.1:p.Gln170His
NM_001350235.1:c.510G>T	NP_001337164.1:p.Gln170His
NM_005026.4:c.510G>T	NP_005017.3:p.Gln170His
XM_006710687.2:c.510G>T	XP_006710750.1:p.Gln170His
XM_006710689.2:c.510G>T	XP_006710752.1:p.Gln170His
XM_017001476.1:c.510G>T	XP_016856965.1:p.Gln170His
XM_017001477.1:c.510G>T	XP_016856966.1:p.Gln170His
XM_017001478.1:c.510G>T	XP_016856967.1:p.Gln170His
XM_017001479.1:c.510G>T	XP_016856968.1:p.Gln170His
XM_017001480.1:c.510G>T	XP_016856969.1:p.Gln170His
XM_017001481.1:c.510G>T	XP_016856970.1:p.Gln170His
XM_017001482.2:c.510G>T	XP_016856971.1:p.Gln170His
XM_017001483.2:c.510G>T	XP_016856972.1:p.Gln170His
XM_024447661.1:c.510G>T	XP_024303429.1:p.Gln170His
XM_024447663.1:c.510G>T	XP_024303431.1:p.Gln170His
XM_024447664.1:c.510G>T	XP_024303432.1:p.Gln170His
XR_002956806.1:n.719G>T
NM_001350234.2:c.510G>T	NP_001337163.1:p.Gln170His
NM_005026.5:c.510G>T MANE Select	NP_005017.3:p.Gln170His